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8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies
The dihydroneopterin aldolase (DHNA, EC 4.1.2.25) activity of FolB protein is required for the conversion of 7,8-dihydroneopterin (DHNP) to 6-hydroxymethyl-7,8-dihydropterin (HP) and glycolaldehyde (GA) in the folate pathway. FolB protein from Mycobacterium tuberculosis (MtFolB) is essential for bac...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993393/ https://www.ncbi.nlm.nih.gov/pubmed/33752554 http://dx.doi.org/10.1080/14756366.2021.1900157 |
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author | Czeczot, Alexia de Matos Roth, Candida Deves Ducati, Rodrigo Gay Pissinate, Kenia Rambo, Raoní Scheibler Timmers, Luís Fernando Saraiva Macedo Abbadi, Bruno Lopes Macchi, Fernanda Souza Pestana, Víctor Zajaczkowski Basso, Luiz Augusto Machado, Pablo Bizarro, Cristiano Valim |
author_facet | Czeczot, Alexia de Matos Roth, Candida Deves Ducati, Rodrigo Gay Pissinate, Kenia Rambo, Raoní Scheibler Timmers, Luís Fernando Saraiva Macedo Abbadi, Bruno Lopes Macchi, Fernanda Souza Pestana, Víctor Zajaczkowski Basso, Luiz Augusto Machado, Pablo Bizarro, Cristiano Valim |
author_sort | Czeczot, Alexia de Matos |
collection | PubMed |
description | The dihydroneopterin aldolase (DHNA, EC 4.1.2.25) activity of FolB protein is required for the conversion of 7,8-dihydroneopterin (DHNP) to 6-hydroxymethyl-7,8-dihydropterin (HP) and glycolaldehyde (GA) in the folate pathway. FolB protein from Mycobacterium tuberculosis (MtFolB) is essential for bacilli survival and represents an important molecular target for drug development. S8-functionalized 8-mercaptoguanine derivatives were synthesised and evaluated for inhibitory activity against MtFolB. The compounds showed IC(50) values in the submicromolar range. The inhibition mode and inhibition constants were determined for compounds that exhibited the strongest inhibition. Additionally, molecular docking analyses were performed to suggest enzyme-inhibitor interactions and ligand conformations. To the best of our knowledge, this study describes the first class of MtFolB inhibitors. |
format | Online Article Text |
id | pubmed-7993393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-79933932021-03-31 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies Czeczot, Alexia de Matos Roth, Candida Deves Ducati, Rodrigo Gay Pissinate, Kenia Rambo, Raoní Scheibler Timmers, Luís Fernando Saraiva Macedo Abbadi, Bruno Lopes Macchi, Fernanda Souza Pestana, Víctor Zajaczkowski Basso, Luiz Augusto Machado, Pablo Bizarro, Cristiano Valim J Enzyme Inhib Med Chem Research Paper The dihydroneopterin aldolase (DHNA, EC 4.1.2.25) activity of FolB protein is required for the conversion of 7,8-dihydroneopterin (DHNP) to 6-hydroxymethyl-7,8-dihydropterin (HP) and glycolaldehyde (GA) in the folate pathway. FolB protein from Mycobacterium tuberculosis (MtFolB) is essential for bacilli survival and represents an important molecular target for drug development. S8-functionalized 8-mercaptoguanine derivatives were synthesised and evaluated for inhibitory activity against MtFolB. The compounds showed IC(50) values in the submicromolar range. The inhibition mode and inhibition constants were determined for compounds that exhibited the strongest inhibition. Additionally, molecular docking analyses were performed to suggest enzyme-inhibitor interactions and ligand conformations. To the best of our knowledge, this study describes the first class of MtFolB inhibitors. Taylor & Francis 2021-03-23 /pmc/articles/PMC7993393/ /pubmed/33752554 http://dx.doi.org/10.1080/14756366.2021.1900157 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Czeczot, Alexia de Matos Roth, Candida Deves Ducati, Rodrigo Gay Pissinate, Kenia Rambo, Raoní Scheibler Timmers, Luís Fernando Saraiva Macedo Abbadi, Bruno Lopes Macchi, Fernanda Souza Pestana, Víctor Zajaczkowski Basso, Luiz Augusto Machado, Pablo Bizarro, Cristiano Valim 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies |
title | 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies |
title_full | 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies |
title_fullStr | 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies |
title_full_unstemmed | 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies |
title_short | 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies |
title_sort | 8-mercaptoguanine-based inhibitors of mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993393/ https://www.ncbi.nlm.nih.gov/pubmed/33752554 http://dx.doi.org/10.1080/14756366.2021.1900157 |
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